Chromium complexes and their use in olefin polymerization

ABSTRACT

A composition having the formula I  
                 
     where R 1  and R 2  are independently hydrogen, C 1  to C 12  linear and branched alkyl, C 3  to C 12  cycloalkyl, aryl, C 1  to C 12  alkoxy, F, Cl, SO 3 , C 1  to C 12  perfluoroalkyl, and N(CH 3 ) 2 ,    R 3  is independently selected from the group consisting of hydrogen, C 1  to C 12  linear and branched alkyl, C 3  to C 12  cycloalkyl, aryl, and 2,2,2-trifluoroethyl,    A is —C(R 4 )—, —(CH 2 ) x —, —(CH 2 ) x NH(CH 2 ) x —, or —CY 2 CY 2 —,    where R 4  is a hydrocarbyl, halosubstituted hydrocarbyl, or alkoxy group of from 1 to 12 carbon atoms, x is an integer from 1 to 12, and Y is halogen, and X is halogen, triflate, acetate, trifluoroacetate, hydride, or tetrafluoroborate. When combined with an activating co-catalyst is useful in polymerizing olefinic monomers.

This application claims the benefit of U.S. Provisional Application No.60/583,881 filed Jun. 29, 2004.

FIELD OF INVENTION

The present invention is directed toward chromium complexes and theiruse in olefin polymerization. More specifically the invention isdirected toward chromium trihalide complexes having bis-benzimidazoleligands and their use in olefin polymerization.

BACKGROUND OF INVENTION

Nitrogen-based chelates of transition metals such as Ti, Ni, Pd, Co andFe have been actively investigated in recent years as olefinpolymerization catalysts. Those incorporating bidentate α-diimine andtridentate bisminopyridine ligands have been found to be highly activecatalysts for olefin polymerization.

More recently, similar investigations of coordination chemistry andcatalysis have been extended to chromium (III) complexes containingcertain imidizole-based chelate ligands. These complexes, when activatedwith methyl aluminoxane (“MAO”) were found to catalyze theoligomerization of ethylene. (See Ruther et al, Organometallics, 2001,20, 1247-1250).

Despite the advances made in catalyst systems employing chromium, thereis a continuing need for new catalysts that will provide a greaterdegree of control over polymerization processes. Homogenous,chromium-based catalysts are believed to possess the potential ofproviding better control over polymerization processes than many otherorganometallic catalysts. For example, a neutral nickel (II) catalystcontaining bidentate monoanionic ligands produce linear α-olefins with avery wide range Schulz-Flory type distribution. An object of the presentinvention, therefore, is to provide novel chromium based catalystsuseful in the polymerization of olefins.

SUMMARY OF INVENTION

In one embodiment the invention is a composition having the formula

-   where R¹ and R² are independently hydrogen, C₁ to C₁₂ linear and    branched alkyl, C₃ to C₁₂ cycloalkyl, aryl, C₁ to C₁₂ alkoxy, F, Cl,    SO₃, C₁ to C₁₂ perfluoroalkyl, and N(CH₃)₂,-   R³ is independently selected from the group consisting of hydrogen,    C₁ to C₁₂ linear and branched alkyl, C₃ to C₁₂ cycloalkyl, aryl, and    2,2,2-trifluoroethyl,-   A is —C(R⁴)—, —(CH₂)_(x)—, —(CH₂)_(x)NH(CH₂)_(x)—, or —CY₂CY₂—,-   where R⁴ is a hydrocarbyl, halosubstituted hydrocarbyl, or alkoxy    group of from 1 to 12 carbon atoms, x is an integer from 1 to 12,    and Y is halogen, and-   X is halogen, triflate, acetate, trifluoroacetate, hydride, or    tetrafluoroborate.

In another embodiment the invention is a catalyst comprising thereaction product of a compound of formula I and an activatingco-catalyst.

In yet another embodiment a method for making polyolefins is providedwhich includes contacting olefinic monomers under polymerizationconditions with a catalyst composition comprising a composition havingformula I and an activating co-catalyst.

These and other features, aspects and advantages of the presentinvention will become better understood with regard to the followingdescription and appended claims.

DETAILED DESCRIPTION

The invention provides novel chromium bis-benzimidazole complexes which,when used with an activating co-catalyst, provides a novel catalystcomposition.

The chromium complexes of the invention are represented by the formula

-   where R¹ and R² are independently, hydrogen, C₁ to C₁₂ linear and    branched alkyl, C₃ to C₁₂ cycloalkyl, and aryl, C₁ to C₁₂ alkoxy, F,    Cl, SO₃, C₁ to C₁₂ perfluoroalkyl, and N(CH₃)₂,-   R³ is independently selected from the group consisting of hydrogen,    C₁ to C₁₂ linear and branched alkyl, C₃ to C₁₂ cycloalkyl, aryl, and    2,2,2-trifluoroethyl,-   A is —C(R⁴)—, —(CH₂)_(x)—, —(CH₂)_(x)NH(CH₂)_(x)—, or —CY₂CY₂—,-   where R⁴ is a hydrocarbyl, halosubstituted hydrocarbyl, or alkoxy    group of from 1 to 12 carbon atoms, x is an integer from 1 to 12,    and Y is halogen, and-   X is halogen, triflate, acetate, trifluoroacetate, hydride, or    tetrafluoroborate.

Preferred compositions are those in which R³ is an alkyl group,especially n-butyl; where R¹ and R² are hydrogen or methyl; where A is—C(C₄H₉)—, or —CF₂CF₂—; and X is chlorine.

The compounds of the invention are made by reacting Cr(III) halide,e.g., CrCl₃ or CrCl₃.(THF)₃ (THF=tetrahydrofuran), with the appropriateligand. This is done by adding the chromium compound to a solvent ordiluent and then adding the ligand to the solvent or diluent. Suitablesolvents or diluents include liquid or supercritical gases such as CO₂,tetrahydrofuran, straight and branched alkanes like isobutane, butane,pentane, hexane and mixtures thereof; cyclic and alicyclic hydrocarbonslike cyclohexane, methylcyclohexane; halogenated hydrocarbons such aschlorobenzene; perfluorinated C₄₋₁₀ alkanes; and aromatic hydrocarbonslike toluene. The resulting chromium complex is separated by removal of,or precipitation from, the diluent or solvent.

Optionally, the chromium complex may be prepared in the solvent ordiluent to be used for the polymerization. In this instance, thechromium complex and the co-catalyst are typically combined in thesolvent or diluent used for the polymerization immediately before addingthe olefinic monomer to be polymerized.

As indicated the following ligands are preferred:1,1′-bis(1-butylbenzimidazol-2-yl)pentane;1,2-bis(1-butylbenzimidazol-2-yl)-1,1,2,2-tetrafluoroethane; and1,1′-bis(1-butyl-4-methylbenzimidazol-2-yl)pentane.

1,1′-Bis(1-butylbenzimidazol-2-yl)pentane has the structure II:

1,2-Bis(1-butylbenzimidazol-2-yl)-1,1,2,2 tetrafluoroethane has thestructure III:

1,1′-Bis(1-butyl-4 methyl benzimidazol-2-yl)pentane has the structureIV:

The ligands of the invention may be synthesized using techniques knownto those skilled in the art. In this regard, see for example, U.S. Pat.No. 6,037,297, herein incorporated by reference.

The chromium compositions of the invention are combined with anactivating co-catalyst to provide a catalyst useful in polymerizingolefins. Examples of such co-catalysts include aluminum compoundscontaining an Al—O bond such as the alkylalumoxanes, of which methylalumoxane (“MAO”) is an example. Other suitable co-catalysts includemixtures of alkyl alumoxane with one or more trialkyl aluminum ortrialkyl boron compounds, and mixtures of alkyl alumoxanes with aluminumhalides or boron halides and an alkylating agent. Examples of alkylatingagents include methyl magnesium chloride and methyl lithium. Typicallythe alkyl group will range from 1 to about 12 carbon atoms.

A preferred activating co-catalyst is methylalumoxane.

Olefinic monomers that are useful in forming polymers with the catalystof the invention include, for example, ethylenically unsaturatedmonomers, non-conjugated dienes, oligomers and higher molecular weight,vinyl terminated macromers. Representative examples include C₂₋₂₀olefins, vinylcyclohexane, tetrafluoroethylene, and mixtures thereof.Preferred are C₂₋₁₀ α-olefins such as ethylene and 1-hexene.

In general the polymerization is accomplished at temperatures rangingfrom about −100° C. to 250° C., preferably 0° C. to 250° C., andpressures of from atmospheric to 2000 atmospheres (200 Mpa). Suitablepolymerization conditions include those known to be useful for olefinpolymerization catalysts when activated by aluminum or boron compounds.Suspension, solution, slurry, gas phase or other process conditions maybe employed if desired.

The polymerization typically will be conducted in the presence of asolvent. Suitable solvents include toluene, methylene chloride,chlorobenzene, THF, and the like.

The polymerization will be conducted for a time sufficient to form thepolymer and the polymer is recovered by techniques known in the art andillustrated in the examples hereinafter.

In the following examples involving ligands and catalysts, stage meltingpoints were determined visually and are uncorrected. DSC melting pointswere taken with a TA Instruments 2920 calorimeter using a scan rate of10° C./minute. Elemental analyses were carried out by QTI, Whitehouse,N.J. Field desorption mass spectra were obtained on a VG-ZAB system.Infrared spectra were obtained on a Mattson Galaxy Series 5000spectrometer running First software. NMR spectra were obtained using aBruker Avance 400 Ultrashield spectrometer, with default calibration toCFCl₃ used as a standard for ¹⁹F spectra. Solid-state NMR experimentswere carried out using a Chemagnetics CMXII-200 spectrometer.

EXAMPLE 1 Synthesis of 1,1′-bis(1-butylbenzimidazol-2-yl)pentane(TriBu-BBIM)

In a 250 mL 35/25 ball joint flask, 1,2-phenylenediamine (54 mmol) wascombined with malonic acid (2 equivalents). Polyphosphoric acid (˜100 g)was added directly to the solid mixture. The flask was fitted with anair-driven mechanical stirring shaft and heated to 160° C. under anitrogen purge maintained with a septum and needle. The molten mixturewas stirred for 7 hours and subsequently poured slowly into a large (1L) excess of cold water. A Waring™ blender was used to grind the solidproduct/water slurry. The water was then neutralized to a pH of ˜8 withammonium hydroxide. The product,1,1′-bis(1-butylbenzimidazol-2-yl)pentane, was isolated by filtrationand dried in a vacuum oven at 110° C. for several days. A 23.00 g (0.093mol) quantity of this product was placed in a 300 mL round bottom flaskwith a side arm. This was followed by the addition of 25 mL of anhydrousDMSO. The flask was then fitted with a bubbler. Under a flow ofnitrogen, 6.0 g of sodium hydride (60% dispersion in mineral oil) wasadded over one hour while stirring at 0° C. The reaction was allowed towarm to room temperature, and 25.00 mL (0.220 mol) of 1-iodobutane wasadded dropwise over one hour. The reaction mixture was left stirringunder nitrogen for 48 hours. The reaction mixture was quenched withwater and then an additional 400 mL of water was added. After stirringfor one half hour, a biphasic solution was obtained. The organic layerwas extracted with cyclohexane and was washed with water. The volatileswere removed from the cyclohexane phase under reduced pressure to leavea dark oil. The oil was chromatographed on silica gel with methylenechloride as the eluent. The solvent was removed under reduced pressurefrom the combined eluents to give a very pale-pink oil that crystallizedupon standing at room temperature (C₂₇H₃₆N₄, FW=416.61). Yield: 20.44 g(67%). ¹H NMR (CDCl₃): δ 7.79 (m, 2H), 7.24 (m, 6H), 4.88 (t, J=7.9 Hz,1H), 4.16 (dsp, J=5.0 Hz, J=40.9 Hz, 4H), 2.59 (m, 2H), 1.44 (m, 4H),1.16 (m, 4H), 1.10 (m, 2H), 0.99 (m, 2H), 0.89 (t, J=6.8 Hz, 3H), 0.61(t, J=7.0 Hz, 6H). ¹³C NMR (CDCl₃): δ 151.8, 142.4, 135.6, 122.6, 122.0,119.6, 109.7, 44.0, 40.9, 31.5, 31.2, 30.1, 22.5, 20.0, 14.0, 13.4. IR(KBr pellet, cm⁻¹): 3050 (m), 2955 (m), 2931 (m), 2862 (m), 1613 (w),1501 (m), 1458 (s), 1400 (s), 1331 (m), 1285 (m), 1008 (m), 933 (m), 743(s), 434 (w). R_(f)=0.73 (ethyl acetate). FD-MS m/z (%): 416.1 (M⁺).Melting point (stage) 82-83° C.

EXAMPLE 2 Synthesis of [1,1′-bis(1-butylbenzimidazol-2-yl)pentane]CrCl₃((TriBu-BBIM)CrCl₃) (A)

CrCl₃.(THF)₃ (0.27 g, 0.72 mmol) was weighed into a flask equipped witha stirrer under argon. THF (15 mL) was added to the flask followed bythe ligand triBu-BBIM (0.33 g, 0.79 mmol). The solution was stirredovernight at room temperature. At the end of this time period, thesolution was added to 100 mL of diethyl ether. The precipitate wasfiltered and washed with ether and hexane and dried under vacuum at roomtemperature. Yield: 0.4 g, 87% (C₂₇H₃₆N₄CrCl₃, FW=574.96). NMR spectrain CDCl₃ and THF showed broad peaks, indicating a paramagnetic center.IR (KBr pellet, cm⁻¹): 2959.0 (s), 2872.2 (m), 1614.5 (m), 1597.2 (w),1494.9 (s), 1479.5 (s), 1460.2 (s), 1435.1 (m), 1375.3 (w), 1338.7 (w),1275.0 (m), 750.3 (s). Melting point (stage) 215° C.

EXAMPLE 3 Synthesis of1,2-bis(1-butylbenzimidazol-2-yl)-1,1,2,2-tetrafluoroethane(DiBu-(C₂F₄)-BBIM)

In a 250 mL 35/25 ball joint flask, 1,2-phenylenediamine (5.92 g, 54.7mmol) was combined with tetrafluorosuccinic acid (5.2 g, 27.36 mmol).Polyphosphoric acid (83 g) was added directly to the solid mixture. Theflask was fitted with an air-driven mechanical stirring shaft and heatedto 160° C. under a nitrogen purge maintained with a septum and needle.The molten mixture was stirred for 7 hours and subsequently pouredslowly into a large (1 L) excess of cold water. A Waring™ blender wasused to grind the solid product/water slurry. The water was thenneutralized to a pH of ˜8 with ammonium hydroxide. The brown particulateproduct, 1,2-bis(benzimidazol-2-yl)-1,1,2,2-tetrafluoroethane, wasisolated by filtration, dried in a vacuum oven, ground to a fine powderwith a mortar and pestle, and once again slurried in ca. 1 L water whichwas then neutralized to pH 8 with ammonium hydroxide. The solid wasagain collected by filtration and dried under diffusion pump vacuum at110° C. for several days (7.96 g, 87%; C₁₆H₁₀F₄N₄, FW=334.27). A smallamount of water was still present by ¹H NMR (br s, 3.35 ppm). ¹H NMR(d₆-DMSO): δ 13.66 (br s, 2H, NH), 7.67 and 7.34 (each br s, 4H, arylC—H. ¹³C{¹H} NMR (solid state): δ 142.2, 135.5 (C—N), 124.2, 120.2,114.4 (aryl) (C═N and CF₂ not observed). ¹⁹F NMR (d₆-DMSO, vs. CFCl₃):δ−110.61. IR (KBr pellet, cm⁻¹): 3063 (m), 3011 (m), 2947 (m), 2864 (s),2749 (s), 2699 (sh), 2647 (s), 2546 (m), 2527 (m), 1942 (w), 1903 (w),1778 (w), 1622 (w), 1591 (m), 1537 (w), 1492 (m), 1456 (s), 1441 (s),1389 (w), 1317 (m), 1279 (m), 1231 (m), 1202 (w), 1161 (vs), 1140 (vs),1030 (m), 1014 (m), 999 (m), 941 (m), 909 (m), 887 (m), 789 (w), 766(w), 739 (s), 675 (w), 619 (w), 590 (m), 545 (w), 434 (m). Elementalanalysis calculated for C₁₆H₁₀F₄N₄: C, 57.49; H, 3.02; F, 22.73; N,16.76. Found: C, 56.74; H, 2.82; F, 21.95; N, 16.70. FD-MS m/z (%): 334(M⁺, 100), 167 (C₈H₅F₂N₂, 6). Melting point (DSC, maximum): 383° C.

Subsequently, 1,2-bis(benzimidazol-2-yl)-1,1,2,2-tetrafluoroethane (4.02g, 12.03 mmol) was degassed on a vacuum line in a 250 mL round-bottomedflask and flushed with argon. Anhydrous, nitrogen-sparged DMSO (135 mL)was cannulated into the flask, resulting in a purple solution.Separately, a 500 mL three-necked flask equipped with a stirbar,addition funnel, vacuum adapter, and a septum was assembled in the glovebox. Sodium hydride (powder, 1.15 g, 48.10 mmol) was added, and theflask was placed under argon on a Schlenk line. Anhydrous DMSO (35 mL)was added via cannula to form a slurry. The bis-benzimidazole solutionwas then cannulated into the addition funnel and added dropwise to thesodium hydride slurry over a 30 minute period at 0° C., giving a cloudyblack solution. The reaction mixture was warmed to room temperature overa 2 hour period and sparged iodobutane (8.86 g, 48.12 mmol) was added.The slurry was stirred overnight at room temperature and the resultantclear amber, viscous solution was poured into 300 mL of deionized water.The organic products were isolated by extraction with 3×200 mL ofcyclohexane, followed by back-extraction of the combined organic layerswith 1×200 mL deionized water. Removal of cyclohexane gave 4.725 g (88%)of the light tan product,1,2-bis(1-butylbenzimidazol-2-yl)-1,1,2,2-tetrafluoroethane, which wasrecrystallized from methanol at −10° C. (3.795 g, 71%; C₂₄H₂₆F₄N₄,FW=446.48). ¹H NMR (CDCl₃): δ 7.80 (d, J=8.1 Hz, 2H), 7.44 (d, J=8.1 Hz,2H), 7.38 (tr, J=7.5 Hz, 2H), 7.31 (tr, J=7.6 Hz, 2H) (aryl), 4.39 (tr,J=7.8 Hz, 4H, CH₂N), 1.87 (5, J=7.8 Hz, 4H, CH ₂CH₂N), 1.44 (6, J=7.5Hz, 4H, CH ₂CH₃), 0.96 (tr, J=7.36, 6H, CH ₃). ¹³C{¹H} NMR (CDCl₃,assigned by DEPT): δ 141.63 (aryl C—N), 140.89 (tr, J_(CF)=28.4 Hz,C═N), 135.40 (aryl C—N), 124.53 and 122.95 (aryl o- to C—N), 121.11(aryl m- to C—N), 112.84 (tr of tr, J_(CF)=253.4 and 34.4 Hz, CF₂),110.39 (aryl m- to C—N), 45.27 (CH₂N), 32.07 (CH₂CH₂N), 19.94 (CH₂CH₃),13.46 (CH₃). ¹⁹F NMR (CDCl₃, vs. CFCl₃): δ−107.52. IR (KBr pellet,cm⁻¹): 3082 (w), 3055 (m), 3017 (m), 2965 (s), 2936 (s), 2874 (s), 2737(w), 1939 (w), 1896 (w), 1861 (w), 1811 (w), 1771 (w), 1734 (w), 1682(w), 1615 (m), 1588 (m), 1499 (s), 1487 (s), 1464 (sh), 1452 (vs), 1424(s), 1373 (s), 1335 (s), 1283 (w), 1248 (s), 1227 (m), 1167 (vs), 1142(vs), 1101 (vs), 1005 (m), 980 (w), 963 (w), 916 (s), 893 (s), 783 (m),739 (vs), 669 (m), 598 (m), 548 (w), 440 (m). Elemental analysiscalculated for C₂₄H₂₆F₄N₄: C, 64.56; H, 5.87; F, 17.02; N, 12.55. Found:C, 64.32; H, 5.77; F, 16.93; N, 12.46. Melting point (stage): 112° C.FD-MS m/z (%): 446 (M⁺, 100).

EXAMPLE 4 Synthesis of[1,2-bis(1-butylbenzimidazol-2-yl)-1,1,2,2-tetrafluoroethane]CrCl₃(DiBu-(C₂F₄)-BBIM)CrCl₃) (B)

THF (5 mL) was added to DiBu-(C₂F₄)-BBIM (0.381 g, 0.053 mmol) in anargon-flushed 250 mL round-bottomed flask. The ligand was only partiallysoluble resulting in a slurry. CrCl₃.(THF)₃ (0.32 g, 0.853 mmol) in THF(10 mL) was added to the slurry. The mixture was stirred overnight atroom temperature. Subsequently, methylene chloride (5 mL) was added andthe resulting purple solution was stirred for 2 days. All solvents werethen removed under vacuum, and the solids were washed with diethyletherand hexane and dried under vacuum at room temperature to give[1,2-bis(1-butylbenzimidazol-2-yl)-1,1,2,2-tetrafluoroethane]CrCl₃ as alight purple solid (0.52 g, 60%, C₂₄H₂₆F₄N₄CrCl₃, FW=604.84). IR (KBrpellet, cm⁻¹): 3010 (s), 2890 (s), 1599.1 (s) .1498.8 (s), 1487.2 (s),1452.5 (s), 1425.5 (s), 1373.4 (s), 1334.8 (s), 1248.0 (s), 1226.8 (m),1167.0 (s), 1141.9 (s), 1103.4 (s), 1045.5 (w), 1006.9 (m), 962.5 (w),916.2 (w), 993.1 (w), 862.2 (s), 796.7 (w), 744.6 (s). Melting point(stage) 125° C.

EXAMPLE 5 Synthesis of 1,1-bis(1-butyl-4-methylbenzimidazol-2-yl)pentane(TriBu-4,4′-diMe-BBIM)

The ligand precursor bis(4-methyl-2-benzimidazolyl)methane was firstprepared in a procedure analogous to that given for1,2-bis(benzimidazol-2-yl)-1,1,2,2-tetrafluoroethane in Example 3. Thereagents used were: 2,3-diaminotoluene (15.26 g, 0.125 moles), malonicacid (6.53 g, 0.063 moles), and polyphosphoric acid (40 g). Uponheating, the contents of the flask had the viscosity of milk and turneda deep bluish purple color. The compoundbis(4-methyl-2-benzimidazolyl)methane was isolated as a purple bluesolid (11.35 g, 66% yield, C₁₇H₁₆N₄, FW=276.32). ¹H NMR (d₆-DMSO): δ7.30 (d, J=7.9 Hz, 2H), 7.03 (tr, J=7.6, 2H), 6.94 (d, J=7.2, 2H) (arylCH), 4.46 (s, 2H, CH ₂), 2.50 (s, theoretical 12H, Me). ¹H NMR (CDCl₃):δ 7.30 (d, J=8), 7.04 (t, J=8), 6.94 (d, J=8) (aryl), 4.48 (s, CH ₂),2.49 (s, Me). ¹H NMR (d₇-DMF): 7.35 (d, J=8.0, 2H), 7.05 (t, J=7.6, 2H),6.96 (d, J=7.0, 2H) (aryl), 4.59 (br s, 2H, CH ₂), 2.51 (s, 6H, Me).¹³C{¹H} NMR (d₆-DMSO, assigned by DEPI): δ 149.73 (C═N), 138.39, 138.01(br, aryl C—N), 124.50 (aryl C-Me), 121.93, 121.58, 111.98 (aryl C—H),29.35 (CH₂), 16.80 (CH₃). ¹³C{¹H} NMR (CDCl₃): δ 150.1 (C═N), 138.7,138.4 124.8, 121.9, 121.6 112.3 (aryl carbons), 29.7 (bridging CH₂),17.1 (CH₃ on phenyl rings). IR (KBr pellet, cm⁻¹): 3377 (s), 3169 (sh),3022 (s), 2918 (s), 2857 (sh), 2745 (s), 2693 (sh), 1904 (w), 1829 (w),1761 (w), 1620 (w), 1533 (m), 1439 (vs), 1418 (sh), 1319 (w), 1277 (m),1231 (m), 1157 (w), 1078 (w), 1022 (w), 783 (m), 745 (s). Elementalanalysis calculated for C₁₇H₁₆N₄: C, 73.89; H, 5.84; N, 20.27. Found: C,69.57; H, 5.49; N, 19.28 (incomplete combustion; calculated C:H:N ratio12.7:1.0:3.5; found C:H:N ratio 12.7:1.0:3.5). FD-MS m/z (%): 277 (M⁺,100); 291 (13%, assigned as impurity with backbone CH₂ oxidized to C═O).Melting point (stage): appears to decompose by darkening, 145-165° C.Melting point (DSC, maximum): 282° C. (broad).

Subsequently, bis(4-methyl-2-benzimidazolyl)methane (10.0 g, 36.2 mmol)was reacted with NaH (3.47 g, 145 mmol) and iodobutane (12.4 mL, 20.1 g,109 mmol) in anhydrous DMSO following a procedure analogous to theprocedure given for1,2-bis(1-butylbenzimidazol-2-yl)-1,1,2,2-tetrafluoroethane in Example3. Following extraction, the burgundy-black product mixture (14.04 g,87%) was eluted in batches through a silica gel column using 90:10CH₂Cl₂/ethyl acetate. The collected product (R_(f)˜0.7) was notcompletely separable from impurities at R_(f)˜0.25-0.30 and the solventfront, and was subsequently eluted through a large neutral aluminacolumn (J. T. Baker Type IB; 41 mm ID; stationary phase height ˜40 cm)using CH₂Cl₂. Following elution of a yellow byproduct, the pure ligandwas collected as a red oil (R_(f)˜0.74, 6.00 g, 37%) and dried at 60° C.under high vacuum (C₂₉H₄₀N₄, FW=444.65). ¹H NMR (CDCl₃): δ 7.12-7.01 (m,6H, aryl), 4.90 (t, J=7.8 Hz, 1H, backbone C H), 4.16 (m, 4H, butyl CH₂N), 2.68 (s, 6H, aryl CH₃), 2.57 (br apparent q, J=7.7 Hz, 2H, backbonebutyl CH ₂CH), 1.45-1.43 (m, 4H), 1.20-1.15 (m, 4H), 1.04-0.95 (br m,4H) (butyl CH ₂), 0.90 (t, J=7.0 Hz, 3H, backbone butyl CH₃), 0.61 (t,J=7.3 Hz, 6H, N-butyl CH ₃). ¹³C{¹H} NMR (CDCl₃, assigned by DEPT): δ151.23 (C═N), 141.76 and 135.23 (aryl C—N), 129.58 (aryl C-Me), 122.23,122.17, 107.10 (aryl), 44.01 (CH₂N), 40.96 (backbone CH), 31.47 (N-butylCH₂), 31.12, 30.12, 22.65 (backbone butyl CH₂), 20.00 (N-butyl CH₂),16.70 (aryl CH₃), 13.97 (backbone butyl CH₃), 13.33 (N-butyl CH₃. IR(thin film on NaCl, cm⁻¹): 3055 (w, 3027 (w), 2957 (vs), 2932 (vs), 2873(m), 1733 (w), 1601 (w), 1502 (m), 1459 (s), 1431 (s), 1399 (s), 1379(m), 1366 (m), 1335 (m), 1268 (m), 1241 (m), 1215 (w), 1152 (w), 1115(w), 1075 (w), 1037 (w), 970 (w), 947 (w), 904 (w), 872 (w), 780 (m),749 (s) cm⁻¹. Elemental analysis calculated for C₂₉H₄₀N₄: C, 78.33; H,9.07; N, 12.60. Found: C, 78.14; H, 9.03; N, 12.44. FD-MS m/z (%): 444(M⁺, 100).

EXAMPLE 6 Synthesis of[1,1-bis(1-butyl-4-methylbenzimidazol-2-yl)pentane]CrCl₃((TriBu-4,4′-diMe-BBIM)CrCl₃) (C)

This material was prepared following a procedure analogous to example 4.The reagents used were TriBu-4,4′-diMe-BBIM (0.561 g, 1.26 mmol, solublein THF) and CrCl₃.(THF)₃ (0.473 g, 1.26 mmol).[1,1-Bis(1-butyl-4-methylbenzimidazol-2-yl)pentane]CrCl₃ was isolated asa light purple solid (0.45 g, 95%, C₂₉H₄₀N₄CrCl₃, FW=603.01). IR (KBrpellet, cm⁻¹): 1602.9 (s), 1531.6 (w), 1489.1(m), 1456.3 (m), 1043.6(m), 1010.8 (s), 920.1 (w), 862.2(s), 781.2 (w), 748.4 (w). Meltingpoint (stage): 115° C.

EXAMPLE 7 Polymerizations

99.9% pure ethylene (Grade 4.5, 99.995%, BOC Gases) was used asreceived. Methyl aluminoxane (30 wt % solution in toluene) was used asreceived from Albemarle. Toluene used as a solvent was dried by passingthrough purification columns of copper catalyst to remove oxygen andalumina to remove moisture (Pangborn, A. B.; Giardello, M. A.; Grubbs,R. H.; Rosen, R. K.; Timmers, F. J. Organometallics 1996, 15,1518-1520). The polymer products were characterized by ¹H, and ¹³C NMRusing a Varian INOVA 300 spectrometer with a 5 mm switchable broadbandprobe. Molecular weights were determined using a Waters Associates 150CHigh Temperature gel permeation chromatography chromatograph equippedwith three Polymer Laboratories mixed bed Type B columns in1,2,4-trichlorobenzene at 135° C., using a Waters DRI detector and apolyethylene calibration curve.

Polymerizations were run in a 300 mL Parr™ reactor fitted with amechanical stirrer. Catalyst was weighed in a glass liner under argon inthe glove box; then, 75 mL of solvent was added to the catalyst. Thereactor was then sealed and brought out of the glove box and attached tothe ethylene feed. The specified amount of methyl aluminoxane solutionwas added to the reactor after dissolving ethylene in the solution atatmospheric pressure. The pressure was then increased to that specifiedfor the run and the temperature for the run was set. At the end of thereaction, excess ethylene was vented, and the reaction was quenched withmethanol. After cooling, the polymer was isolated by precipitation intoacidic methanol, followed by drying under vacuum. Conditions and resultsare summarized in Table 1. TABLE 1 Activity, Kg of mmol Cr:Al Temp Time,C₂H₄, Product/ MW (×10³), Ex. No. Catalyst catalyst ratio Solvent ° C.hr psig mol of Cr MWD ^(a) 7-1 A 0.035 1:500 Toluene 50 24 500 40 151,4.4 7-2 A 0.035 1:300 Toluene 50 24 500 13 140, 8.5 (1 g of 1- hexeneadded) 7-3 A 0.035 1:300 CH₂Cl₂ 50 20 500 507 120, 6.6 7-4 A 0.017 1:260C₆H₅Cl 50 20 500 124 86, 8.1 7-5 A 0.017 1:260 C₆H₅Cl 24 2 100 95 157,24.7 7-6 A 0.017 1:260 CH₂Cl₂ 24 2 100 142 108, 25.6 7-7 A 0.017 1:260Toluene 24 2 100 19 337, 57.7 (bimodal) 7-8 C 0.017 1:260 Toluene 22 2100 8 7-9 B 0017 1:260 Toluene 25 2 100 2^(a) Mw = weight-average molecular weight. MWD = Mw/Mn (Mn =number-average molecular weight)

1. A composition represented by the formula:

where R¹ and R² are independently hydrogen, C₁ to C₁₂ linear andbranched alkyl, C₃ to C₁₂ cycloalkyl, aryl, C₁ to C₁₂ alkoxy, F, Cl,SO₃, C₁ to C₁₂ perfluoroalkyl, and N(CH₃)₂, R³ is independently selectedfrom the group consisting of hydrogen, C₁ to C₁₂ linear or branchedalkyl, C₃ to C₁₂ cycloalkyl, aryl, and 2,2,2-trifluoroethyl, A is—C(R⁴)—, —(CH₂)_(x)—, —(CH₂)_(x)NH(CH₂)_(x)—, or —CY₂CY₂—, where R⁴ is ahydrocarbyl, halosubstituted hydrocarbyl, or alkoxy group of from 1 to12 carbon atoms, x is an integer from 1 to 12, and Y is halogen, and Xis halogen, triflate, acetate, trifluoroacetate, hydride, ortetrafluoroborate.
 2. The composition of claim 1 wherein A is alkyl; R³is alkyl; and X is chlorine.
 3. The composition of claim 2 wherein R¹and R² are hydrogen.
 4. The composition of claim 2 wherein R¹ and R² aremethyl.
 5. The composition of claims 3 and 4 wherein A is a C₅ alkyl andR³ is a C₄ alkyl.
 6. The composition of claim 1 wherein R¹ and R² arehydrogen; R³ is alkyl; A is perhalogenated alkyl; and X is chlorine. 7.The composition of claim 6 wherein R³ is a C₄ alkyl and A is —CF₂CF₂—.8. A catalyst composition comprising the reaction product of: (a) acompound represented by the formula:

and (b) an activating co-catalyst. where R¹ and R² are independentlyhydrogen, C₁ to C₁₂ linear and branched alkyl, C₃ to C₁₂ cycloalkyl,aryl, C₁ to C₁₂ alkoxy, F, Cl, SO₃, C₁ to C₁₂ perfluoroalkyl, andN(CH₃)₂, R³ is independently selected from the group consisting ofhydrogen, C₁ to C₁₂ linear or branched alkyl, C₃ to C₁₂ cycloalkyl,aryl, and 2,2,2-trifluoroethyl, A is —C(R⁴)—, —(CH₂)_(x)—,—(CH₂)_(x)NH(CH₂)_(x)—, or —CY₂CY₂—, where R⁴ is a hydrocarbyl,halosubstituted hydrocarbyl, or alkoxy group of from 1 to 12 carbonatoms, x is from 1 to 12, and Y is halogen, and X is halogen, triflate,acetate, trifluoroacetate, hydride, or tetrafluoroborate.
 9. Thecatalyst composition of claim 8 wherein the activating co-catalyst isselected from the group consisting of alkylalumoxanes, mixtures ofalkylalumoxanes with one or more trialkyl aluminum or trialkyl boroncompounds, and mixtures of alkylalumoxanes with aluminum halides orboron halides and an alkylating agent.
 10. The catalyst composition ofclaim 9 wherein A is alkyl; R³ is alkyl; and X is chlorine.
 11. Thecatalyst composition of claim 10 wherein R¹ and R² are hydrogen.
 12. Thecatalyst composition of claim 10 wherein R¹ and R² are methyl.
 13. Thecatalyst composition of claims 11 and 12 wherein A is a C₅ alkyl and R³is a C₄ alkyl.
 14. The catalyst composition of claim 9 wherein R¹ and R²are hydrogen; R³ is alkyl; A is perhalogenated alkyl; and X is chlorine.15. The catalyst composition of claim 14 wherein R³ is a C₄ alkyl and Ais —CF₂CF₂—.
 16. A method for polymerizing olefinic monomers comprisingcontacting an olefinic monomer or monomers under polymerizationconditions with a catalyst composition comprising the reaction productof: (a) a compound represented by the formula:

and (b) an activating co-catalyst. where R¹ and R² are independentlyhydrogen, C₁ to C₁₂ linear and branched alkyl, C₃ to C₁₂ cycloalkyl,aryl, C₁ to C₁₂ alkoxy, F, Cl, SO₃, C₁ to C₁₂ perfluoroalkyl, andN(CH₃)₂, R³ is independently selected from the group consisting ofhydrogen, C₁ to C₁₂ linear or branched alkyl, C₃ to C₁₂ cycloalkyl,aryl, and 2,2,2-trifluoroethyl, A is —C(R⁴)—, —(CH₂)_(x)—,—(CH₂)_(x)NH(CH₂)_(x)—, or —CY₂CY₂—, where R⁴ is a hydrocarbyl,halosubstituted hydrocarbyl, or alkoxy group of from 1 to 12 carbonatoms, x is an integer from 1 to 12, and Y is halogen, and X is halogen,triflate, acetate, trifluoroacetate, hydride, or tetrafluoroborate. 17.The method of claim 16 wherein the activating co-catalyst is selectedfrom the group consisting of alkylalumoxanes, mixtures of alkylalumoxanes with one or more trialkyl aluminum or trialkyl boroncompounds, and mixtures of alkylalumoxanes with aluminum halides orboron halides and an alkylating agent.
 18. The method of claim 17wherein A is alkyl; R³ is alkyl; and X is chlorine.
 19. The method ofclaim 18 wherein R¹ and R² are hydrogen.
 20. The method of claim 18wherein R¹ and R² are methyl.
 21. The method of claim 19 and 20 whereinA is a C₅ alkyl and R³ is a C₄ alkyl.
 22. The method of claim 17 whereinR¹ and R² are hydrogen; R³ is alkyl; A is perhalogenated alkyl; and X ischlorine.
 23. The method of claim 17 wherein R³ is a C₄ alkyl and A is—CF₂CF₂—.